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Therapeutic effects of amniotic fluid-derived mesenchymal stromal cells on lung injury in rats with emphysema

BACKGROUND: In chronic obstructive pulmonary disease (COPD), two major pathological changes that occur are the loss of alveolar structure and airspace enlargement. To treat COPD, it is crucial to repair damaged lung tissue and regenerate the lost alveoli. Type II alveolar epithelial cells (AECII) pl...

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Autores principales: Li, Yaqing, Gu, Chao, Xu, Wulin, Yan, Jianping, Xia, Yingjie, Ma, Yingyu, Chen, Chun, He, Xujun, Tao, Houquan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201761/
https://www.ncbi.nlm.nih.gov/pubmed/25319435
http://dx.doi.org/10.1186/s12931-014-0120-3
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author Li, Yaqing
Gu, Chao
Xu, Wulin
Yan, Jianping
Xia, Yingjie
Ma, Yingyu
Chen, Chun
He, Xujun
Tao, Houquan
author_facet Li, Yaqing
Gu, Chao
Xu, Wulin
Yan, Jianping
Xia, Yingjie
Ma, Yingyu
Chen, Chun
He, Xujun
Tao, Houquan
author_sort Li, Yaqing
collection PubMed
description BACKGROUND: In chronic obstructive pulmonary disease (COPD), two major pathological changes that occur are the loss of alveolar structure and airspace enlargement. To treat COPD, it is crucial to repair damaged lung tissue and regenerate the lost alveoli. Type II alveolar epithelial cells (AECII) play a vital role in maintaining lung tissue repair, and amniotic fluid-derived mesenchymal stromal cells (AFMSCs) possess the characteristics of regular mesenchymal stromal cells. However, it remains untested whether transplantation of rat AFMSCs (rAFMSCs) might alleviate lung injury caused by emphysema by increasing the expression of surfactant protein (SP)A and SPC and inhibiting AECII apoptosis. METHODS: We analyzed the phenotypic characteristics, differentiation potential, and karyotype of rAFMSCs, which were isolated from pregnant Sprague–Dawley rats. Moreover, we examined the lung morphology and the expression levels of SPA and SPC in rats with emphysema after cigarette-smoke exposure and intratracheal lipopolysaccharide instillation and rAFMSC transplantation. The ability of rAFMSCs to differentiate was measured, and the apoptosis of AECII was evaluated. RESULTS: In rAFMSCs, the surface antigens CD29, CD44, CD73, CD90, CD105, and CD166 were expressed, but CD14, CD19, CD34, and CD45 were not detected; rAFMSCs also strongly expressed the mRNA of octamer-binding transcription factor 4, and the cells could be induced to differentiate into adipocytes and osteocytes. Furthermore, rAFMSC treatment up-regulated the levels of SPA, SPC, and thyroid transcription factor 1 and inhibited AECII apoptosis, and rAFMSCs appeared to be capable of differentiating into AECII-like cells. Lung injury caused by emphysema was alleviated after rAFMSC treatment. CONCLUSIONS: rAFMSCs might differentiate into AECII-like cells or induce local regeneration of the lung alveolar epithelium in vivo after transplantation and thus could be used in COPD treatment and lung regenerative therapy.
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spelling pubmed-42017612014-10-19 Therapeutic effects of amniotic fluid-derived mesenchymal stromal cells on lung injury in rats with emphysema Li, Yaqing Gu, Chao Xu, Wulin Yan, Jianping Xia, Yingjie Ma, Yingyu Chen, Chun He, Xujun Tao, Houquan Respir Res Research BACKGROUND: In chronic obstructive pulmonary disease (COPD), two major pathological changes that occur are the loss of alveolar structure and airspace enlargement. To treat COPD, it is crucial to repair damaged lung tissue and regenerate the lost alveoli. Type II alveolar epithelial cells (AECII) play a vital role in maintaining lung tissue repair, and amniotic fluid-derived mesenchymal stromal cells (AFMSCs) possess the characteristics of regular mesenchymal stromal cells. However, it remains untested whether transplantation of rat AFMSCs (rAFMSCs) might alleviate lung injury caused by emphysema by increasing the expression of surfactant protein (SP)A and SPC and inhibiting AECII apoptosis. METHODS: We analyzed the phenotypic characteristics, differentiation potential, and karyotype of rAFMSCs, which were isolated from pregnant Sprague–Dawley rats. Moreover, we examined the lung morphology and the expression levels of SPA and SPC in rats with emphysema after cigarette-smoke exposure and intratracheal lipopolysaccharide instillation and rAFMSC transplantation. The ability of rAFMSCs to differentiate was measured, and the apoptosis of AECII was evaluated. RESULTS: In rAFMSCs, the surface antigens CD29, CD44, CD73, CD90, CD105, and CD166 were expressed, but CD14, CD19, CD34, and CD45 were not detected; rAFMSCs also strongly expressed the mRNA of octamer-binding transcription factor 4, and the cells could be induced to differentiate into adipocytes and osteocytes. Furthermore, rAFMSC treatment up-regulated the levels of SPA, SPC, and thyroid transcription factor 1 and inhibited AECII apoptosis, and rAFMSCs appeared to be capable of differentiating into AECII-like cells. Lung injury caused by emphysema was alleviated after rAFMSC treatment. CONCLUSIONS: rAFMSCs might differentiate into AECII-like cells or induce local regeneration of the lung alveolar epithelium in vivo after transplantation and thus could be used in COPD treatment and lung regenerative therapy. BioMed Central 2014-10-16 2014 /pmc/articles/PMC4201761/ /pubmed/25319435 http://dx.doi.org/10.1186/s12931-014-0120-3 Text en © Li et al.; licensee BioMed Central Ltd. 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Li, Yaqing
Gu, Chao
Xu, Wulin
Yan, Jianping
Xia, Yingjie
Ma, Yingyu
Chen, Chun
He, Xujun
Tao, Houquan
Therapeutic effects of amniotic fluid-derived mesenchymal stromal cells on lung injury in rats with emphysema
title Therapeutic effects of amniotic fluid-derived mesenchymal stromal cells on lung injury in rats with emphysema
title_full Therapeutic effects of amniotic fluid-derived mesenchymal stromal cells on lung injury in rats with emphysema
title_fullStr Therapeutic effects of amniotic fluid-derived mesenchymal stromal cells on lung injury in rats with emphysema
title_full_unstemmed Therapeutic effects of amniotic fluid-derived mesenchymal stromal cells on lung injury in rats with emphysema
title_short Therapeutic effects of amniotic fluid-derived mesenchymal stromal cells on lung injury in rats with emphysema
title_sort therapeutic effects of amniotic fluid-derived mesenchymal stromal cells on lung injury in rats with emphysema
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4201761/
https://www.ncbi.nlm.nih.gov/pubmed/25319435
http://dx.doi.org/10.1186/s12931-014-0120-3
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